Atlas FDA

BIOPLEX 2200 MMRV IGG

FDA 510(k) clearance K091616 · decided 2010-03-29

Clearance details

K-number
K091616
Device name
BIOPLEX 2200 MMRV IGG
Applicant
Bio-Rad Laboratories
Decision
Substantially Equivalent
Date received
2009-06-03
Decision date
2010-03-29
Days to decision
299 days
Clearance type
Traditional
Product code
OPL
Device class
2
Regulation number
866.3510
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Redmond, WA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
DYNEX SmartPLEX MMRV IgG Assay Kit (K212769)Dynex Technologies, Inc.2023-09-29
BIOPLEX 2200 MMRV IGG IT ON BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM, BIOPLEX 2200 MMRV IGG CALIBRATOR SET, AND BIOPL (K111072)Bio-Rad Laboratories2011-08-23

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
MONOLISA ANTI-HBS EIA (P050048/S010)Bio-Rad Laboratories2025-04-18
BIO-RAD MONOLISA ANTI-HBS EIA (P050048/S009)Bio-Rad Laboratories2013-12-12
BIO-RAD MONOLISA ANTI-HBS EIA (P050048/S008)Bio-Rad Laboratories2012-11-13
BIO-RAD MONOLISA ANTI-HBS EIA AND MONOLISA ANTI-HBS CALIBRATOR KIT (P050048/S007)Bio-Rad Laboratories2012-11-13
BIO-RAD MONOLISA ANTI-HBS EIA (P050048/S004)Bio-Rad Laboratories2011-04-25
MONOLISA ANTI-HBS EIA AND MONOLISA ANTI-HBS CALIBRATOR KIT (P050048/S005)Bio-Rad Laboratories2010-11-23
BIO-RAD MONOLISA ANTI -HBS EIA (P050048/S006)Bio-Rad Laboratories2010-09-27
BIO-RAD MONOLISA ANTI-HBS EIA (P050048/S002)Bio-Rad Laboratories2010-03-12